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      Organic carbon isotopes in terrestrial Permian-Triassic boundary sections of North China: Implications for global carbon cycle perturbations

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          Abstract

          The end-Permian mass extinction (ca. 252 Ma) represents the most severe biotic crisis of the Phanerozoic, and it was accompanied by profound environmental perturbations, especially to the global carbon cycle, as indicated by sharp negative carbon isotope excursions (CIE) in both carbonates (δ13Ccarb) and organic matter (δ13Corg). To date, carbon isotope records are mostly from marine Permian-Triassic transitional sequences with relatively few high-resolution carbon isotope profiles having been generated for terrestrial facies. Terrestrial Permian-Triassic sequences suitable for high-resolution carbon isotope study are rare globally and are difficult to correlate with better-studied marine sequences. However, carbon isotope records from continental facies are essential to a full understanding of global carbon cycle changes during the Permian-Triassic transition. Here, we present bulk δ13Corg profiles for three terrestrial sections in North China representing Permian-Triassic transitional beds. These profiles exhibit similar patterns of secular variation defining three stages: (1) a pre-CIE interval, (2) a CIE interval, characterized by a rapid negative shift of 1.7‰–2.2‰ within the middle part of the Sunjiagou Formation, and (3) a post-CIE interval. The similarity of the CIE in all three study sections facilitates correlations among them, and its presence in the Permian-Triassic transitional beds suggests that it is equivalent to the negative CIE at the Permian-Triassic boundary in the Meishan global stratotype section and point (GSSP) and in coeval marine and terrestrial sections globally. The end-Permian CIE was probably triggered by a massive release of 13C-depleted carbon from volcanogenic sources leading to elevated atmospheric pCO2, although oceanic sources of CO2 cannot be ruled out at present.

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          Preservation of elemental and isotopic source identification of sedimentary organic matter

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            Interpreting carbon-isotope excursions: carbonates and organic matter

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              Carbon isotope compositions of terrestrial C3 plants as indicators of (paleo)ecology and (paleo)climate.

              A broad compilation of modern carbon isotope compositions in all C3 plant types shows a monotonic increase in δ(13)C with decreasing mean annual precipitation (MAP) that differs from previous models. Corrections for temperature, altitude, or latitude are smaller than previously estimated. As corrected for altitude, latitude, and the δ(13)C of atmospheric CO(2), these data permit refined interpretation of MAP, paleodiet, and paleoecology of ecosystems dominated by C3 plants, either prior to 7-8 million years ago (Ma), or more recently at mid- to high latitudes. Twenty-nine published paleontological studies suggest preservational or scientific bias toward dry ecosystems, although wet ecosystems are also represented. Unambiguous isotopic evidence for C4 plants is lacking prior to 7-8 Ma, and hominid ecosystems at 4.4 Ma show no isotopic evidence for dense forests. Consideration of global plant biomass indicates that average δ(13)C of C3 plants is commonly overestimated by approximately 2‰.
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                Author and article information

                Journal
                GSA Bulletin
                Geological Society of America
                0016-7606
                1943-2674
                October 16 2019
                May 01 2020
                October 16 2019
                May 01 2020
                : 132
                : 5-6
                : 1106-1118
                Affiliations
                [1 ]State Key Laboratory of Biogeology and Environmental Geology, School of Earth Sciences, China University of Geosciences, Wuhan 430074, China
                [2 ]State Key Laboratory of Geological Processes and Mineral Resources, China University of Geosciences, Wuhan 430074, China
                [3 ]Department of Geology, University of Cincinnati, Cincinnati, Ohio 45221-0013, USA
                [4 ]Department of Earth and Environmental Studies, Montclair State University, Montclair, New Jersey 07043, USA
                Article
                10.1130/B35228.1
                f0574d6c-112e-4b1a-a642-180c2f60a77c
                © 2020
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